ratiotx
Senior Radioanalytical Development Scientist
Boston, Massachusetts · Senior
Sponsorship not specifiedDetected 12 days ago
Project ManagementGMPFDA RegulatoryResearchMass SpectrometryMicrosoft Office
About the role
- About Ratio Therapeutics Ratio Therapeutics is committed to improving and extending the lives of cancer patients without sacrificing their quality of life.
- Join us in our quest to become the leading innovator in radioligand therapy and improve the lives of cancer patients and their families.
- About the Position Ratio is seeking a Senior Scientist, Analytical Development to join our growing team of scientists.
Responsibilities
- Independently develop and optimize analytical quality control methods (such as HPLC, TLC, LC-MS and GC) to support advancement of Ratio's lead compounds.
- Lead the transition of early-phase analytical method development to methods appropriate for technology transfer. Lead the transition of early phase methods into GMP/GLP appropriate QC methods.
- Design and execute phase-appropriate analytical strategies, including method qualification/verification/validation suitable for tech transfer and regulatory submissions.
- Lead analytical method training for quality control personnel in analytical techniques, data interpretation and best practices to ensure consistent execution and data integrity.
- Support OOS/OOT and deviation investigations, identify root causes and implement corrective and preventive actions related to analytical methods and instrumentation.
- Lead the transition of early-phase analytical method development to methods appropriate for technology transfer.
- Lead the transition of early phase methods into GMP/GLP appropriate QC methods.
- In this role, the successful candidate will be responsible for analytical method development to support GMP method development and technology transfer.
- The ideal candidate has a track-record of successful GMP technology development, enjoys working in a collaborative and fast-paced environment, and will seek to maintain trustworthy relationships with interdisciplinary teams at partner organizations.
Requirements
- Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites.
- Experience with project management (experience managing external CROs or CDMOs is an asset).
Compensation
- The annual base salary for this role is expected to range between $145,000 and $165,000.
Benefits
- Prior experience with radioactive materials such as radiopharmaceuticals and medical isotopes is required.
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